Label: MOSAIC INSTANT HAND SANITIZER WITH MOISTURIZING FORMULA- alcohol gel

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated April 4, 2020

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

View All Sections
  • ACTIVE INGREDIENT

    Active ingredient                                  Purpose

    Ethyl Alcohol                62%      ...        Antiseptic

  • PURPOSE

    Hand sanitizer to help decrease bacteria on the skin.

  • KEEP OUT OF REACH OF CHILDREN

    Children must be supervised in use of this product.

  • INDICATIONS & USAGE

    keep out of eyes

    when water, soap and towel are not available

  • WARNINGS

    For external use only.
    Flammable. Keep away from hear or flame.

    Do not apply around eyes; Do not use in ears and mouth. When using this products, avoid contact with eyes. In case of contact, flush eyes with water.

    Stop using and ask a doctor, if redness and irritation develop and persist for more than 72 hours.

    OTHER INFORMATION: store at 20 Celsius Degree (68 - 77 Fahrenheit), may discolor fabrics.

  • DOSAGE & ADMINISTRATION

    Pump as needed into your palms and thoroughly spread on both hands, and rub the skin until dry. 

    Children must be supervised in use of this product.

  • INACTIVE INGREDIENT

    Water, Glycerin, Aloe Barbadensis gel, Carbomer, Fragrance

  • PRINCIPAL DISPLAY PANEL

    image of label

  • INGREDIENTS AND APPEARANCE
    MOSAIC INSTANT HAND SANITIZER WITH MOISTURIZING FORMULA 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52174-106
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    alcohol (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) alcohol62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CARBOMER 934 (UNII: Z135WT9208)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52174-106-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product04/04/2020
    2NDC:52174-106-0260 mL in 1 BOTTLE; Type 0: Not a Combination Product04/04/2020
    3NDC:52174-106-03237 mL in 1 BOTTLE; Type 0: Not a Combination Product04/04/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/04/2020
    Labeler - Ningbo BST Clean And Care Products Co., Ltd (529352816)
    Registrant - Ningbo BST Clean And Care Products Co., Ltd (529352816)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo BST Clean And Care Products Co., Ltd529352816manufacture(52174-106)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials

More Info on this Drug

Get Label RSS Feed, View NDC Code(s)NEW!